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91445

Sigma-Aldrich

10,12-Tricosadiynoic acid

≥98.0% (GC)

Sinónimos:

Tricosa-10,12-diynoic acid

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About This Item

Fórmula empírica (notación de Hill):
C23H38O2
Número de CAS:
66990-30-5
Peso molecular:
346.55
Beilstein:
1880414
Número MDL:
MFCD00041683
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
57653435
NACRES:
NA.22

Análisis

≥98.0% (GC)

formulario

crystals

condiciones de almacenamiento

protect from light

mp

56-60 °C

cadena SMILES

CCCCCCCCCCC#CC#CCCCCCCCCC(O)=O

InChI

1S/C23H38O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23(24)25/h2-10,15-22H2,1H3,(H,24,25)

Clave InChI

DIEDVCMBPCRJFQ-UHFFFAOYSA-N

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Descripción general

10,12-Tricosadiynoic acid, also known as Tricosa-10,12-diynoic acid, is a monomeric amphiphilic diacetylene fatty acid characterized by long paraffinic chains on both sides of the diacetylene moiety. This compound is often used in the synthesis of polymerizable monolayers and Langmuir-Blodgett multilayers.

Aplicación

  • Acid-responsive color transition in polymer assemblies: 10,12-Tricosadiynoic acid is employed in the development of acid-responsive polydiacetylene-Na(+) assemblies, showcasing a unique red-to-blue color transition. This property is significant for applications in smart sensors and visual indicators in various industrial processes (Saymung et al., 2024).
  • Colorimetric sensing capabilities: The synthesis of polydiacetylene vesicles incorporating 10,12-Tricosadiynoic acid demonstrates their utility as colorimetric sensors. This application is particularly valuable in the detection of microbial peptides, contributing to advancements in food safety and pharmaceutical analysis (Yadav and Tiwari, 2021).

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Lars Hoff et al.
Journal of surfactants and detergents, 14(4), 585-593 (2011-10-01)
The ultrasound contrast agents Echovist(®) and Levovist(®) (Bayer AG, Schering AG, Germany) are based on the release of gas bubbles from milled α-d-galactose. In diagnostic ultrasound, for this class of contrast agents, there is a need for prolonged contrast duration.
Solid-state polymerization of tricosa-10, 12-diynoic acid
Tieke B, et al.
Journal of Materials Science, 17, 1156-1166 (1982)
Max Weston et al.
Analytica chimica acta, 1148, 238190-238190 (2021-02-01)
The incorporation of colorimetric sensors as quality indicators in food packaging is an exciting new area of research that could improve food management. The standard approach, however, demands a reliable interface between the sensor and the food and risks food
Congcong Gu et al.
The Analyst, 145(8), 3049-3055 (2020-03-07)
Surface modification of gold nanoparticles (AuNPs) has significant and complicated effects on their interactions with cell membranes. In this study, we used a lipid/polyacetylene (PDA) vesicle sensor as the lipid membrane model to evaluate AuNP-lipid membrane interactions. Based on the
Guan-Lin Wu et al.
Toxins, 12(4) (2020-04-25)
It is widely accepted that snake venom cardiotoxins (CTXs) target the plasma membranes of cells. In the present study, we investigated the role of Asp residues in the interaction of Naja atra cardiotoxin 1 (CTX1) and cardiotoxin 3 (CTX3) with
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